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Nanofibrillar cellulose as a Lyoprotective
Matrix in The Freeze-Drying of HepG2
Liver Cancer Cells
INTRODUCTION
Freeze-drying of complex human cells has yielded insufficient viabilities dueto the lack of compatible lyoprotective matrices [1]. The usage ofnanofibrillar cellulose (NFC) as a lyoprotective matrix is not defined inprevious literature. The aim of this thesis is to study the effects of NFC whenit is freeze-dried and recreated while carrying 3D cell spheroid systems.
OBJECTIVES
We have evaluated the capabilities of NFC as a lyoprotective matrix in thefreeze-drying process of HepG2 cells under sterile conditions. The highestviability was reached trough optimization of the process itself and testing ofmost suitable compounds for cryo- and lyopreservation (5).
METHODS
A human liver carcinoma cell line HepG2 was cultivated in a mixture of NFCand medium (1) and then freeze-dried and stored in controlled conditions(3). Simultaneously, HepG2 control samples without NFC were freeze-driedand stored in corresponding manner. After rehydration, the viability of bothsample types was measured (4) and the mitochondrial activity evaluated. Inaddition, the morphology of the cells during each step was analyzed (2, 6).
RESULTS
Results demonstrate that without the protective NFC matrix the HepG2 cellscould not survive the freeze-drying process. However, when protected by theNFC matrix, the cells gained noticeable viability when rehydrated.
CONCLUSIONS
Nanofibrillar cellulose appears to be a promising candidate as alyoprotective matrix in the freeze-drying of human cells. The preservedviability during the freeze-drying could lead to the development of new cellproducts for research and clinical applications in the future.
Vili-Veli Auvinen1,
Arto Merivaara1,
Raili Koivuniemi1,
Heli Paukkonen1,
Patrick Laurén1,
Timo Laaksonen*1,2,
Marjo Yliperttula*1
1 Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, P.O. Box 56, FI-00014 Helsinki, Finland
2 Department of Chemistry and Bioengineering, Tampere University of Technology, P.O. Box 541, FI-33101 Tampere, Finland
* Corresponding author
HELSINGIN YLIOPISTO
HELSINGFORS UNIVERSITET
UNIVERSITY OF HELSINKI
FARMASIAN TIEDEKUNTA
FARMACEUTISKA FAKULTETEN
FACULTY OF PHARMACY
ACKNOWLEDGEMENTS
This work was funded by the University of Helsinki. The authorsacknowledge the Drug Discovery and Chemical Biology Network andInstitute of Biotechnology, funded by Biocenter Finland, for providing accessto screening instrumentation, and the Helsinki Electron microscopy unit atthe Institute of Biotechnology, University of Helsinki, for the electronmicroscopy. Tekes, Finnish Center for Innovation, is acknowledged via theUniversity driven 3D-Nano-MiniT Tekes project and UPM-Kymmene Oyj isacknowledged for providing the nanofibrillated cellulose for the Tekes-project and the present study.
RESULTS
1. 2. 3.
4. 5.
References
[1] Wikström, J. (2013). Alginate-based microencapsulation and lyophilization of human retinal pigment epithelial cell line (ARPE-19) for cell therapy.
Optimization of Lyoprotectants
PEG 6000 (0.7 wt.%)
Trehalose(0.3 wt.%)
Glycerol (1 wt.%)
Viability (Calcein intensity)
GrowDex® 0.8 wt.% & 24h trehal. incub. x x x ++
GrowDex® 0.8 wt.% & 24h trehal. incub. x x +
GrowDex® 0.8 wt.% & 24h trehal. incub. x +GrowDex® 0.8 wt.% & 24h trehal. incub. x ++GrowDex® 0.8 wt.% & 24h trehal. incub. x x ++GrowDex® 0.8 wt.% & 24h trehal. incub. +
GrowDex® 0.4 wt.% & 24h trehal. incub. x x x +++
GrowDex® 0.4 wt.% & 24h trehal. incub. x x ++
GrowDex® 0.4 wt.% & 24h trehal. incub. x ++GrowDex® 0.4 wt.% & 24h trehal. incub. x ++GrowDex® 0.4 wt.% & 24h trehal. incub. x x +++GrowDex® 0.4 wt.% & 24h trehal. incub. ++GrowDex® 0.8 wt.% x x +GrowDex® 0.8 wt.% x +GrowDex® 0.8 wt.% +Without GrowDex® x xWithout GrowDex® x xWithout GrowDex® xWithout GrowDex® & 24h treha. Incub. x xWithout GrowDex® & 24h treha. Incub. x xWithout GrowDex® & 24h treha. Incub. x
6.
Day 5 HepG2 spheroids before freeze-drying
Live Dead After freeze-drying and rehydration